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QC Microbiologist

Eagle Labs, Inc

Job Description

Job Description

Quality Control Microbiology Supervisor

Overview:

Quality Control (QC) Microbiology Supervisor oversees daily microbiology laboratory operations and a team of analysts. They ensure all testing—such as sterility, bioburden, endotoxin, and environmental monitoring—complies with strict adherence to the GMP regulations. This role spans method validation, root-cause investigations, and data integrity verification.

Key Duties:

These are only highlighted by major key duties. Other requested duties assigned by Eagle Labs, Inc for job function by Quality Control Manager, Director of Laboratory Operations, or Executive leadership.

  • Scheduling, conducting OOS (Out-of-Specification) investigations, and managing staff training scheduling, conducting investigations, and managing staff training.
  • Supervises routine testing, including sterility testing, bacterial endotoxins (BET), bioburden, microbial limits, and growth promotion of media.
  • Support assay method verification, transfer, and equipment qualification within the Laboratory.
  • Act as a subject matter expert (SME) during internal audits and regulatory inspections.
  • Lead Out-of-Specification (OOS) investigations, initiate Corrective and Preventive Actions (CAPA), and implement change controls.

Core Responsibilities:

  • Team Leadership & Development: Supervise, train, and mentor laboratory analysts. Manage scheduling, performance evaluations, and gowning/aseptic qualifications.
  • Testing Oversight: Oversee and review routine microbiological assays, including sterility, bioburden, bacterial endotoxins (LAL), microbial identification (e.g., MALDI-TOF), and water testing.
  • Environmental Monitoring (EM): Approve EM data, analyze trending reports, and monitor classified cleanroom utilities to maintain compliance.

Qualifications & Requirements

  • Education: Bachelor’s degree in microbiology, Biology, or a closely related life science discipline.
  • Experience: Minimum 5 years of hands-on experience in a cGMP pharmaceutical or biotech microbiology laboratory, including at least 3 or more years in a lead or supervisory capacity.
  • Technical Skills: Advanced understanding of aseptic processing, cleanroom behaviors, and compendial requirements (USP, EP, JP).
  • Soft Skills: Strong problem-solving, data trending capabilities, and excellent verbal and written communication skills.

Vacancy posted 3 days ago
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